Enzymatic Hydrolysis of the Chemical Warfare Agent VX and its Neurotoxic Analogues by Organophosphorus Hydrolase

Abstract

Organophosphorus hydrolase (OPH) is a bacterial enzyme that hydrolyzes a variety of organophosphorus (OP) neurotoxins, including many widely used pesticides and chemical warfare agents containing P-O, P-F, P-CN and P-S bonds. It has extremely high efficiency in hydrolysis of many different phosphotriester and phosphothiolester pesticides (P-O bond) such as paraoxon (kcat3800s−1) and coumaphos (kcat = 800s−1) or phosphonate (P-F) neurotoxins such as DFP (kcat = 350s−1) and the chemical warfare agent sarin (kcat = 56s−1). In contrast, the enzyme has much lower catalytic capabilities for phosphonothioate neurotoxins such as acephate (kcat = 2.8 s−1) or the chemical warfare agent VX [O-ethyl S-(2-diisopropyl-aminoethyl) methylphosphonothioate] (kcat = 0.3s−1). This lower specificity for VX and its analogues are reflected by the specificity constants (kcat/Km values) for VX = 0.75 × 103 M−1 s−1 compared to 5.5 × 107M−1 s−1 for paraoxon. Different metal-associated forms of the enzyme demonstrated significantly varying hydrolytic capabilities for VX and its analogues, and the activity of OPH (Co+2) was consistently higher than that of OPH (Zn+2) by five to twenty fold. Hydrolysis of the P-S bonds was determined by monitoring the formation of free -SH groups, and the specific cleavage of the P-S bond was verified by 31P NMR analysis.